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2020 – today
- 2020
[j6]Bingbing Zheng
, Yaoqi Liu, Yu Zhu, Fuli Yu, Tianjiao Jiang, Dawei Yang, Tao Xu:
MSD-Net: Multi-Scale Discriminative Network for COVID-19 Lung Infection Segmentation on CT. IEEE Access 8: 185786-185795 (2020)
2010 – 2019
- 2016
- [j5]Zhuoyi Huang, Navin Rustagi, Narayanan Veeraraghavan, Andrew Carroll, Richard A. Gibbs, Eric Boerwinkle, Manjunath Gorentla Venkata, Fuli Yu:
A hybrid computational strategy to address WGS variant analysis in >5000 samples. BMC Bioinform. 17: 361 (2016) - [j4]Dongliang Ding, Dongyue Wu, Fuli Yu:
Spark在人类基因领域的应用 (Application of Spark in Human Genome). 计算机科学 43(Z6): 502-504 (2016) - 2014
- [j3]Jeffrey G. Reid, Andrew Carroll, Narayanan Veeraraghavan, Mahmoud Dahdouli, Andreas Sundquist, Adam C. English, Matthew N. Bainbridge, Simon White, William J. Salerno, Christian Buhay, Fuli Yu, Donna M. Muzny, Richard Daly, Geoff Duyk, Richard A. Gibbs, Eric Boerwinkle:
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline. BMC Bioinform. 15: 30 (2014) - 2013
- [c3]Zhuoyi Huang, Jin Yu, Fuli Yu:
Cloud processing of 1000 genomes sequencing data using Amazon Web Service. GlobalSIP 2013: 49-52 - 2012
- [j2]Danny Challis, Jin Yu, Uday S. Evani, Andrew R. Jackson, Sameer Paithankar, Cristian Coarfa, Aleksandar Milosavljevic, Richard A. Gibbs, Fuli Yu:
An integrative variant analysis suite for whole exome next-generation sequencing data. BMC Bioinform. 13: 8 (2012) - 2011
- [c2]Uday S. Evani, Danny Challis, Jin Yu, Andrew R. Jackson, Sameer Paithankar, Matthew N. Bainbridge, Cristian Coarfa, Aleksandar Milosavljevic, Fuli Yu:
Enabling Atlas2 personal genome analysis on the cloud. GENSiPS 2011: 117-120 - [c1]Yiqi Lu, Yanghua Xiao, Yaoliang Chen, Danfeng Xu, Fuli Yu:
A novel approach for alignments output storage problem facing clinical scenarios. GENSiPS 2011: 174-177 - 2010
- [j1]Cristian Coarfa, Fuli Yu, Christopher A. Miller, Zuozhou Chen, R. Alan Harris, Aleksandar Milosavljevic:
Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing. BMC Bioinform. 11: 572 (2010)
Coauthor Index
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